Investigation of the Effect of 4 in 1 Block Application on Postoperative Analgesia in Knee Surgeries.

NCT ID: NCT04765579

Last Updated: 2021-02-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

62 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-02-20

Study Completion Date

2021-08-20

Brief Summary

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to investigate the effects of ultrasonography-guided 4in1 block application on postoperative analgesia in patients undergoing knee surgery. After knee surgeries performed with spinal anesthesia, 4in1 block will be applied in one group and medical analgesics will be applied in the service in the other group.

Detailed Description

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Conditions

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Visual Analogy Scala

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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4in1

4in1 block will be applied in the operation room

visual analogy scala

Intervention Type BEHAVIORAL

We will investigate the effect of 4in1 block by questioning the vas score of the patients, its effect on quadriceps strength, and additional analgesia needs for 24 hours.

medical

medical analgesics will be applied in the service

visual analogy scala

Intervention Type BEHAVIORAL

We will investigate the effect of 4in1 block by questioning the vas score of the patients, its effect on quadriceps strength, and additional analgesia needs for 24 hours.

Interventions

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visual analogy scala

We will investigate the effect of 4in1 block by questioning the vas score of the patients, its effect on quadriceps strength, and additional analgesia needs for 24 hours.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* ASA I-II
* 18-60 ages
* who were informed about the study and accepted,
* who underwent knee surgery

Exclusion Criteria

* ASA III-IV
* who are under general anesthesia
* who do not agree to participate in the study
* who are urgently operated
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Derince Training and Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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Seyran Köksal

resident

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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Seyran-Tez

Identifier Type: -

Identifier Source: org_study_id

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